Evidence map›Paper›PMID 34753772›Full record

ArticleCancer research2022

Inhibition of FGFR Reactivates IFNγ Signaling in Tumor Cells to Enhance the Combined Antitumor Activity of Lenvatinib with Anti-PD-1 Antibodies.

Yusuke Adachi, Hiroshi Kamiyama, Kenji Ichikawa, Sayo Fukushima, Yoichi Ozawa, Shogo Yamaguchi, Satoshi Goda, Takayuki Kimura, Kotaro Kodama, Masahiro Matsuki and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Cancer research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 118 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
118citing papers in PubMed, 5 pooled it
7.5field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

118 citing papers in PubMed, 5 syntheses or guidelines pooled it, 147 citations in OpenAlex.

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58 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 1 institution in 1 country.

Yusuke AdachiTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki, Japan. y3-adachi@hhc.eisai.co.jp y-funahashi@hhc.eisai.co.jp.
Hiroshi KamiyamaTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki, Japan.
Kenji IchikawaTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki, Japan.
Sayo FukushimaTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki, Japan.
Yoichi OzawaTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki, Japan.
Shogo YamaguchiTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki, Japan.
Satoshi GodaTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki, Japan.
Takayuki KimuraTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki, Japan.
Kotaro KodamaTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki, Japan.
Masahiro MatsukiTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki, Japan.
Saori Watanabe MiyanoTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki, Japan.
Akira YokoiTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki, Japan.
Yu KatoTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki, Japan.ORCID 0000-0003-1662-6983
Yasuhiro FunahashiTsukuba Research Laboratories, Eisai Co., Ltd., Ibaraki, Japan. y3-adachi@hhc.eisai.co.jp y-funahashi@hhc.eisai.co.jp.ORCID 0000-0002-9299-0704
Eisai (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Combination therapies consisting of immune checkpoint inhibitors plus anti-VEGF therapy show enhanced antitumor activity and are approved treatments for patients with renal cell carcinoma (RCC). The immunosuppressive roles of VEGF in the tumor microenvironment are well studied, but those of FGF/FGFR signaling remain largely unknown. Lenvatinib is a receptor tyrosine kinase inhibitor that targets both VEGFR and FGFR. Here, we examine the antitumor activity of anti-PD-1 mAb combined with either lenvatinib or axitinib, a VEGFR-selective inhibitor, in RCC. Both combination treatments showed greater antitumor activity and longer survival in mouse models versus either single agent treatment, whereas anti-PD-1 mAb plus lenvatinib had enhanced antitumor activity compared with anti-PD-1 mAb plus axitinib. Flow cytometry analysis showed that lenvatinib decreased the population of tumor-associated macrophages and increased that of IFNγ-positive CD8

Indexed as

AnimalsAntibodies, MonoclonalAntineoplastic AgentsCarcinoma, HepatocellularCarcinoma, Renal CellCell Line, TumorDisease Models, AnimalDrug SynergismFemaleHumansInterferon-gammaKidney NeoplasmsLiver NeoplasmsMiceMice, Inbred BALB CPhenylurea CompoundsAntibodies, MonoclonalAntineoplastic AgentsIFNG protein, humanIFNG protein, mouseInterferon-gammalenvatinibPdcd1 protein, mousePhenylurea CompoundsProgrammed Cell Death 1 ReceptorProtein Kinase InhibitorsQuinolinesReceptors, Fibroblast Growth Factor

Identifiers

PMID34753772
PMCPMC9397636
OpenAlexW3212668399

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.